Thursday, September 22, 2016

FML


See also: Generic FML Forte Liquifilm


FML is a brand name of fluorometholone ophthalmic, approved by the FDA in the following formulation(s):


FML (fluorometholone - ointment; ophthalmic)



  • Manufacturer: ALLERGAN

    Approval date: September 4, 1985

    Strength(s): 0.1% [RLD]

FML (fluorometholone - suspension/drops; ophthalmic)



  • Manufacturer: ALLERGAN

    Approval date: July 28, 1982

    Strength(s): 0.1% [RLD]

Has a generic version of FML been approved?


No. There is currently no therapeutically equivalent version of FML available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of FML. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with FML.

See also...

  • FML Ointment Consumer Information (Wolters Kluwer)
  • Fluorometholone Consumer Information (Wolters Kluwer)
  • Fluorometholone Acetate Suspension Consumer Information (Wolters Kluwer)
  • Fluorometholone Ointment Consumer Information (Wolters Kluwer)
  • Fluorometholone ophthalmic Consumer Information (Cerner Multum)
  • Fluorometholone AHFS DI Monographs (ASHP)

Furadantin


Furadantin is a brand name of nitrofurantoin, approved by the FDA in the following formulation(s):


FURADANTIN (nitrofurantoin - suspension; oral)



  • Manufacturer: SHIONOGI INC

    Approved Prior to Jan 1, 1982

    Strength(s): 25MG/5ML [RLD][AB]

Has a generic version of Furadantin been approved?


Yes. The following products are equivalent to Furadantin:


nitrofurantoin suspension; oral



  • Manufacturer: AMNEAL PHARMS

    Approval date: May 11, 2011

    Strength(s): 25MG/5ML [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Furadantin. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Furadantin.

See also...

  • Furadantin Suspension Consumer Information (Wolters Kluwer)
  • Furadantin Consumer Information (Cerner Multum)
  • Furadantin Advanced Consumer Information (Micromedex)
  • Nitrofurantoin Consumer Information (Drugs.com)
  • Nitrofurantoin Consumer Information (Wolters Kluwer)
  • Nitrofurantoin Suspension Consumer Information (Wolters Kluwer)
  • Nitrofurantoin Consumer Information (Cerner Multum)
  • Novo-Furan Suspension Advanced Consumer Information (Micromedex)
  • Nitrofurantoin Advanced Consumer Information (Micromedex)
  • Nitrofurantoin AHFS DI Monographs (ASHP)

Visicol


Visicol is a brand name of sodium biphosphate/sodium phosphate, approved by the FDA in the following formulation(s):


VISICOL (sodium phosphate, dibasic anhydrous; sodium phosphate, monobasic, monohydrate - tablet; oral)



  • Manufacturer: SALIX PHARMS

    Approval date: September 21, 2000

    Strength(s): 0.398GM;1.102GM [RLD]

Has a generic version of Visicol been approved?


No. There is currently no therapeutically equivalent version of Visicol available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Visicol. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Non-aqueous colonic purgative formulations
    Patent 5,616,346
    Issued: April 1, 1997
    Inventor(s): Aronchick; Craig A.
    Orally administered colonic purgative formulations and methods of its use for effecting partial or complete purgation of the colon in mammals, the formulations consisting of non-aqueous admixtures of monobasic, dibasic and tribasic sodium phosphates administered in tablet or capsule form in concentrations of from 0.01 to 0.85 grams per kilogram body weight. Preferred embodiments include the addition of binders, dispersants and buffers which do not adversely affect osmolality or effectiveness of the purgative formulations.
    Patent expiration dates:

    • May 18, 2013
      ✓ 
      Patent use: METHOD OF USE OF VISICOL



See also...

  • Visicol Consumer Information (Wolters Kluwer)
  • Visicol Consumer Information (Cerner Multum)
  • Fleet Enema Consumer Information (Wolters Kluwer)
  • Sodium Phosphates Consumer Information (Wolters Kluwer)
  • Sodium Phosphates Enema Consumer Information (Wolters Kluwer)
  • Sodium Phosphates Solution Consumer Information (Wolters Kluwer)
  • Sodium biphosphate and sodium phosphate Consumer Information (Cerner Multum)

Zelapar


Zelapar is a brand name of selegiline, approved by the FDA in the following formulation(s):


ZELAPAR (selegiline hydrochloride - tablet, orally disintegrating; oral)



  • Manufacturer: VALEANT PHARM INTL

    Approval date: June 14, 2006

    Strength(s): 1.25MG [RLD]

Has a generic version of Zelapar been approved?


No. There is currently no therapeutically equivalent version of Zelapar available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Zelapar. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Pharmaceutical and other dosage forms
    Patent 5,648,093
    Issued: July 15, 1997
    Inventor(s): Gole; Dilip J. & Levinson; R. Saul & Wilkinson; Paul K. & Davies; J. Desmond
    Assignee(s): Janssen Pharmaceutica Inc.
    A fast dissolving, solid dosage form defined by a matrix containing gelatin, pectin and/or soy fiber protein and one or more amino acids having from about 2 to 12 carbon atoms is disclosed.
    Patent expiration dates:

    • July 15, 2014
      ✓ 
      Drug product




  • Process for the preparation of a solid pharmaceutical dosage form
    Patent 6,423,342
    Issued: July 23, 2002
    Inventor(s): Andrew William; Jordan & Joy Elaine; Saunders & Patrick; Kearney
    Assignee(s): R. P. Scherer Corporation
    A process for the preparation of a solid pharmaceutical dosage form comprising a carrier and, as active ingredient, a compound which exists, in solution, in an equilibrium between a free acid or free base form and a salt form, and for which there is a difference in volatility between the free acid or free base form and the salt form. The process includes the steps of solidifying a mixture of the compound and carrier in a solvent, and subsequently removing the solvent from the solidified mixture. A pH modifier is added to the mixture prior to solidification to shift the equilibrium to favor the less volatile form of the active ingredient.
    Patent expiration dates:

    • March 1, 2016
      ✓ 
      Drug product



See also...

  • Zelapar Consumer Information (Drugs.com)
  • Zelapar Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Zelapar Consumer Information (Cerner Multum)
  • Zelapar Advanced Consumer Information (Micromedex)
  • Selegiline Consumer Information (Wolters Kluwer)
  • Selegiline Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Selegiline System Consumer Information (Wolters Kluwer)
  • Selegiline Consumer Information (Cerner Multum)
  • Selegiline transdermal Consumer Information (Cerner Multum)
  • Selegiline Advanced Consumer Information (Micromedex)
  • Selegiline Transdermal Advanced Consumer Information (Micromedex)
  • Selegiline Hydrochloride AHFS DI Monographs (ASHP)

Zetia


Zetia is a brand name of ezetimibe, approved by the FDA in the following formulation(s):


ZETIA (ezetimibe - tablet; oral)



  • Manufacturer: MSP SINGAPORE

    Approval date: October 25, 2002

    Strength(s): 10MG [RLD]

Has a generic version of Zetia been approved?


No. There is currently no therapeutically equivalent version of Zetia available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Zetia. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Combinations of hydroxy-substituted azetidinone compounds and HMG CoA Reductase Inhibitors
    Patent 5,846,966
    Issued: December 8, 1998
    Inventor(s): Rosenblum; Stuart B. & Dugar; Sundeep & Burnett; Duane A. & Clader; John W. & McKittrick; Brian A.
    Assignee(s): Schering Corporation
    Hydroxy-substituted azetidinone hypocholesterolemic agents of the formula ##STR1## or a pharmaceutically acceptable salt thereof, wherein: Ar.sup.1 and Ar.sup.2 are aryl or R.sup.4 -substituted aryl; Ar.sup.3 is aryl or R.sup.5 -substituted aryl; X, Y and Z are --CH.sub.2 --, --CH(lower alkyl)-- or --C(dilower alkyl)--; R and R.sup.2 are --OR.sup.6, --O(CO)R.sup.6, --O(CO)OR.sup.9 or --O(CO)NR.sup.6 R.sup.7 ; R.sup.1 and R.sup.3 are H or lower alkyl; q is 0 or 1; r is 0 or 1; m, n and p are 0-4; provided that at least one of q and r is 1, and the sum of m, n, p, q and r is 1-6; and provided that when p is 0 and r is 1, the sum of m, q and n is 1-5; R.sup.4 is selected from lower alkyl, R.sup.5, --CF.sub.3, --CN, --NO.sub.2 and halogen; R.sup.5 is selected from --OR.sup.6, --O(CO)R.sup.6, --O(CO)OR.sup.9, --O(CH.sub.2).sub.1-5 OR.sup.6, --O(CO)NR.sup.6 R.sup.7, --NR.sup.6 R.sup.7, --NR.sup.6 (CO)R.sup.7, --NR.sup.6 (CO)OR.sup.9, --NR.sup.6 (CO)NR.sup.7 R.sup.8, --NR.sup.6 SO.sub.2 R.sup.9, --COOR.sup.6, --CONR.sup.6 R.sup.7, --COR.sup.6, --SO.sub.2 NR.sup.6 R.sup.7, S(O).sub.0-2 R.sup.9, --O(CH.sub.2).sub.1-10 --COOR.sup.6, --O(CH.sub.2).sub.1-10 CONR.sup.6 R.sup.7, --(lower alkylene)COOR.sup.6 and --CH.dbd.CH--COOR.sup.6 ; R.sup.6, R.sup.7 and R.sup.8 are H, lower alkyl, aryl or aryl-substituted lower alkyl; R.sup.9 is lower alkyl, aryl or aryl-substituted lower alkyl; are disclosed, as well as a method of lowering serum cholesterol by administering said compounds, alone or in combination with a cholesterol biosynthesis inhibitor, pharmaceutical compositions containing them, and a process for preparing them.
    Patent expiration dates:

    • September 21, 2013
      ✓ 
      Patent use: TO REDUCE ELEVATED TOTAL-C, APO B, AND NON-HDL-C IN PATIENTS WIHT PRIMARY HYPERLIPIDEMIA BY ADMINISTRATION OF EZETIMIBE IN COMBINATION WITH A STATIN


    • September 21, 2013
      ✓ 
      Patent use: TO REDUCE PLASMA CHOLESTEROL LEVELS IN A MAMMAL


    • September 21, 2013
      ✓ 
      Patent use: TO REDUCE PLASMA CHOLESTEROL LEVELS BY ADMIN EZETIMIBE IN COMBO WITH CHOLESTEROL BIOSYNTHESIS INHIB SELECTED FROM GROUP CONSISTING OF HMG COA REDUCTASE INHIBITORS INCL SIMVASTATIN


    • March 21, 2014
      ✓ 
      Pediatric exclusivity




  • Sterol absorption inhibitor compositions
    Patent 7,030,106
    Issued: April 18, 2006
    Inventor(s): Cho; Wing-Kee Philip
    Assignee(s): Schering Corporation
    The present invention provides compositions, therapeutic combinations and methods including: (a) at least one peroxisome proliferator-activated receptor activator; and (b) at least one substituted azetidinone or substituted β-lactam sterol absorption inhibitor which can be useful for treating vascular conditions, diabetes, obesity and lowering plasma levels of sterols.
    Patent expiration dates:

    • January 25, 2022
      ✓ 
      Drug product


    • July 25, 2022
      ✓ 
      Pediatric exclusivity




  • Methods for inhibiting sterol absorption
    Patent 7,612,058
    Issued: November 3, 2009
    Inventor(s): Cho; Wing-Kee Philip
    Assignee(s): Schering Corporation
    The present invention provides compositions, therapeutic combinations and methods including: (a) at least one peroxisome proliferator-activated receptor activator; and (b) at least one substituted azetidinone or substituted β-lactam sterol absorption inhibitor which can be useful for treating vascular conditions, diabetes, obesity and lowering plasma levels of sterols.
    Patent expiration dates:

    • January 25, 2022
      ✓ 
      Patent use: REDUCTION OF ELEVATED PLASMA STEROL AND/OR STANOL LEVELS IN A MAMMAL


    • January 25, 2022
      ✓ 
      Patent use: TO REDUCE ELEVATED TOTAL-C, LDL-C, APO B AND NON-HDL-C IN PATIENTS WITH PRIMARY HYPERLIPIDEMIA BY ADMINISTRATION OF EZETIMIBE ALONE OR IN COMBINATION WITH A STATIN OR WITH FENOFIBRATE


    • July 25, 2022
      ✓ 
      Pediatric exclusivity




  • Hydroxy-substituted azetidinone compounds useful as hypocholesterolemic agents
    Patent RE37721
    Issued: May 28, 2002
    Inventor(s): Stuart B.; Rosenblum & Sundeep; Dugar & Duane A.; Burnett & John W.; Clader & Brian A.; McKittrick
    Assignee(s): Schering Corporation
    Hydroxy-substituted azetidinone hypocholesterolemic agents of the formula or a pharmaceutically acceptable salt thereof, wherein: Ar1 and Ar2 are aryl or R4-substituted aryl; Ar3 is aryl or R5-substituted aryl; X, Y and Z are —CH2—, —CH(lower alkyl)— or —C(dilower alkyl)—; R and R2 are —OR6, —O(CO)R6, —O(CO)OR9 or —O(CO)NR6R7; R1 and R3 are H or lower alkyl; q is 0 or 1; r is 0 or 1; m, n and p are 0-4; provided that at least one of q and r is 1, and the sum of m, n, p, q and r is 1-6; and provided that when p is O and r is 1, the sum of m, q and n is 1-5; R4 is selected from lower alkyl, R5, —CF3, —CN, —NO2 and halogen R5 is selected from —OR6, —O(CO)R6, —O(CO)OR9, —O(CH2)1-5OR6, —O(CO)NR6R7, —NR6R7, —NR6(CO)R7, —NR6(CO)OR9, —NR6(CO)NR7R8, —NR6SO2R9, —COOR6, —CONR6R7, —COR6, —SO2NR6R7, S(O)0-2R9, —O(CH2)1-10—COOR6, —O(CH2)1-10CONR6R7, —(lower alkylene)COOR6 and —CH═CH—COOR6; R6, R7 and R8 are H, lower alkyl or aryl-substituted Ic R9 is lower alkyl, aryl or aryl-substituted lower alkyl; are disclosed, as well as a method of lowering serum cholesterol by administering said compounds, alone or in combination with a cholesterol biosynthesis inhibitor, pharmaceutical compositions containing them; and a process for preparing them.
    Patent expiration dates:

    • October 25, 2016
      ✓ 
      Patent use: TO REDUCE PLASMA CHOLESTEROL LEVELS IN A MAMMAL
      ✓ 
      Drug substance
      ✓ 
      Drug product


    • April 25, 2017
      ✓ 
      Pediatric exclusivity




  • Hydroxy-substituted azetidinone compounds useful as hypocholesterolemic agents
    Patent RE42461
    Issued: June 14, 2011
    Inventor(s): Rosenblum; Stuart B. & Dugar; Sundeep & Burnett; Duane A. & Clader; John W. & McKittrick; Brian A.
    Assignee(s): Schering Corporation
    Hydroxy-substituted azetidinone hypocholesterolemic agents of the formula or a pharmaceutically acceptable salt thereof, wherein: Ar1 and Ar2 are aryl or R4-substituted aryl; Ar3 is aryl or R5-substituted aryl; X, Y and Z are —CH2—, —CH(lower alkyl)— or —C(dilower alkyl)—; R and R2 are —OR6, —O(CO)R6, —O(CO)OR9 or —O(CO)NR6R7; R1 and R3 are H or lower alkyl; q is 0 or 1; r is 0 or 1; m, n and p are 0-4; provided that at least one of q and r is 1, and the sum of m, n, p, q and r is 1-6; and provided that when p is O and r is 1, the sum of m, q and n is 1-5; R4 is selected from lower alkyl, R5, —CF3, —CN, —NO2 and halogen R5 is selected from —OR6, —O(CO)R6, —O(CO)OR9, —O(CH2)1-5OR6, —O(CO)NR6R7, —NR6R7, —NR6(CO)R7, —NR6(CO)OR9, —NR6(CO)NR7R8, —NR6SO2R9, —COOR6, —CONR6R7, —COR6, —SO2NR6R7, S(O)0-2R9, —O(CH2)1-10—COOR6, —O(CH2)1-10CON6R7, —(lower alkylene)COOR6 and —CH═CH—COOR6; R6, R7 and R8 are H, lower alkyl or aryl-substituted Ic R9 is lower alkyl, aryl or aryl-substituted lower alkyl; are disclosed, as well as a method of lowering serum cholesterol by administering said compounds, alone or in combination with a cholesterol biosynthesis inhibitor, pharmaceutical compositions containing them; and a process for preparing them.
    Patent expiration dates:

    • October 25, 2016
      ✓ 
      Patent use: TO REDUCE ELEVATED TOTAL-C, LDL-C, APO B AND NON-HDL-C IN PATIENTS WITH PRIMARY HYPERLIPIDEMIA BY ADMINISTRATION OF EZETIMIBE ALONE OR IN COMBINATION WITH A STATIN OR WITH FENOFIBRATE
      ✓ 
      Drug substance
      ✓ 
      Drug product


    • October 25, 2016
      ✓ 
      Patent use: TO REDUCE PLASMA CHOLESTEROL LEVELS IN A MAMMAL
      ✓ 
      Drug substance
      ✓ 
      Drug product


    • April 25, 2017
      ✓ 
      Pediatric exclusivity



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • June 5, 2011 - INFORMATION FROM PEDIATRIC STUDIES ADDED TO LABEL

    • December 5, 2011 - PEDIATRIC EXCLUSIVITY

    • January 24, 2015 - CHANGES TO THE PACKAGE INSERT TO REFLECT THE RESULTS OF THE STUDY OF HEART AND RENAL PROTECTION (SHARP) TRIAL

See also...

  • Zetia Consumer Information (Drugs.com)
  • Zetia Consumer Information (Wolters Kluwer)
  • Zetia Consumer Information (Cerner Multum)
  • Zetia Advanced Consumer Information (Micromedex)
  • Zetia AHFS DI Monographs (ASHP)
  • Ezetimibe Consumer Information (Drugs.com)
  • Ezetimibe Consumer Information (Wolters Kluwer)
  • Ezetimibe Consumer Information (Cerner Multum)
  • Ezetimibe Advanced Consumer Information (Micromedex)
  • Ezetimibe AHFS DI Monographs (ASHP)

Flagyl


See also: Generic Flagyl ER


Flagyl is a brand name of metronidazole, approved by the FDA in the following formulation(s):


FLAGYL (metronidazole - capsule; oral)



  • Manufacturer: GD SEARLE LLC

    Approval date: May 3, 1995

    Strength(s): 375MG [RLD][AB]

FLAGYL (metronidazole - tablet; oral)



  • Manufacturer: GD SEARLE LLC

    Approved Prior to Jan 1, 1982

    Strength(s): 250MG [AB], 500MG [RLD][AB]

Has a generic version of Flagyl been approved?


Yes. The following products are equivalent to Flagyl:


metronidazole capsule; oral



  • Manufacturer: ALEMBIC LTD

    Approval date: June 23, 2009

    Strength(s): 375MG [AB]


  • Manufacturer: PAR PHARM

    Approval date: January 29, 2004

    Strength(s): 375MG [AB]

metronidazole tablet; oral



  • Manufacturer: ALEMBIC PHARMS LTD

    Approval date: March 13, 2009

    Strength(s): 250MG [AB], 500MG [AB]


  • Manufacturer: MUTUAL PHARM

    Approval date: July 16, 1986

    Strength(s): 250MG [AB], 500MG [AB]


  • Manufacturer: PLIVA

    Approval date: November 6, 1984

    Strength(s): 250MG [AB]


  • Manufacturer: PLIVA

    Approval date: December 6, 1984

    Strength(s): 500MG [AB]


  • Manufacturer: TEVA

    Approval date: February 8, 1985

    Strength(s): 500MG [AB]


  • Manufacturer: WATSON LABS

    Approval date: September 17, 1982

    Strength(s): 250MG [AB]


  • Manufacturer: WATSON LABS

    Approval date: December 20, 1982

    Strength(s): 500MG [AB]


  • Manufacturer: WATSON LABS

    Approval date: December 20, 1984

    Strength(s): 250MG [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Flagyl. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Flagyl.

See also...

  • Flagyl Consumer Information (Drugs.com)
  • Flagyl Consumer Information (Wolters Kluwer)
  • Flagyl Capsules Consumer Information (Wolters Kluwer)
  • Flagyl Consumer Information (Cerner Multum)
  • Flagyl Oral, Intravenous Advanced Consumer Information (Micromedex)
  • Flagyl AHFS DI Monographs (ASHP)
  • Metronidazole Consumer Information (Drugs.com)
  • Metronidazole Consumer Information (Wolters Kluwer)
  • Metronidazole Capsules Consumer Information (Wolters Kluwer)
  • Metronidazole Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Metronidazole Tablets Consumer Information (Wolters Kluwer)
  • Metronidazole Consumer Information (Cerner Multum)
  • Flagyl I.V. RTU Advanced Consumer Information (Micromedex)
  • Flagyl I.V. RTU Intravenous Advanced Consumer Information (Micromedex)
  • Metronidazole Intravenous Advanced Consumer Information (Micromedex)
  • Metronidazole Oral, Intravenous Advanced Consumer Information (Micromedex)
  • Metronidazole AHFS DI Monographs (ASHP)
  • Metronidazole Hydrochloride AHFS DI Monographs (ASHP)

Zovirax Ointment


Zovirax Ointment is a brand name of acyclovir topical, approved by the FDA in the following formulation(s):


ZOVIRAX (acyclovir - cream; topical)



  • Manufacturer: VALEANT INTL

    Approval date: December 30, 2002

    Strength(s): 5% [RLD]

ZOVIRAX (acyclovir - ointment; topical)



  • Manufacturer: VALEANT INTL

    Approval date: March 29, 1982

    Strength(s): 5% [RLD]

Has a generic version of Zovirax Ointment been approved?


No. There is currently no therapeutically equivalent version of Zovirax Ointment available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Zovirax Ointment. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Zovirax Ointment.

See also...

  • Zovirax Cream Consumer Information (Wolters Kluwer)
  • Zovirax Ointment Consumer Information (Wolters Kluwer)
  • Zovirax Topical Advanced Consumer Information (Micromedex)
  • Zovirax topical AHFS DI Monographs (ASHP)
  • Acyclovir Cream Consumer Information (Wolters Kluwer)
  • Acyclovir Ointment Consumer Information (Wolters Kluwer)
  • Acyclovir topical Consumer Information (Cerner Multum)
  • Acyclovir Topical Advanced Consumer Information (Micromedex)
  • Acyclovir topical AHFS DI Monographs (ASHP)